Linked Data
MyVariant Identifiers:
chr6:g.31236947C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269170C>T , CM000668.2:g.31269170C>T | GRCh38 |
| NC_000006.11:g.31236947C>T , CM000668.1:g.31236947C>T | GRCh37 |
| NC_000006.10:g.31344926C>T | NCBI36 |
| NG_029422.2:g.7962G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.1100G>A MANE Select | ENSP00000365402.5:p.Ter367= | |
| ENST00000376228.9:c.1100G>A | ENSP00000365402.5:p.Ter367= | |
| ENST00000376237.8:c.*687G>A | ENSP00000365412.4:n.*687G>A | |
| ENST00000383329.7:c.1118G>A | ENSP00000372819.3:p.Ter373= | |
| ENST00000466892.5:n.333G>A | ||
| ENST00000470363.5:n.858G>A | ||
| ENST00000487245.5:n.1459G>A | ||
| NM_002117.5:c.1100G>A | NP_002108.4:p.Ter367= | |
| NM_002117.6:c.1100G>A MANE Select | NP_002108.4:p.Ter367= |